Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26750 | A02 | 14961396 | G | A | upstream_gene_variant | MODIFIER | c.-4991G>A| |
S139 |
2 | BAA02g26750 | A02 | 14966511 | G | A | stop_gained | HIGH | c.125G>A|p.Trp42* |
S35 |
3 | BAA02g26750 | A02 | 14966571 | G | A | missense_variant | MODERATE | c.185G>A|p.Gly62Glu |
S223 |
4 | BAA02g26750 | A02 | 14966591 | G | A | missense_variant | MODERATE | c.205G>A|p.Glu69Lys |
S269 |
5 | BAA02g26750 | A02 | 14966664 | C | T | missense_variant | MODERATE | c.278C>T|p.Ser93Phe |
S299 |
6 | BAA02g26750 | A02 | 14966768 | G | A | missense_variant&splice_region_variant | MODERATE | c.302G>A|p.Arg101Lys |
S223 |
7 | BAA02g26750 | A02 | 14967356 | C | T | missense_variant | MODERATE | c.890C>T|p.Ser297Phe |
S226 |
8 | BAA02g26750 | A02 | 14971151 | C | T | downstream_gene_variant | MODIFIER | c.*3578C>T| |
S299 |